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ISAS3Fun方法检测精子顶体完整性的能力及其区分高、低繁殖力公牛的潜力。

Ability of the ISAS3Fun Method to Detect Sperm Acrosome Integrity and Its Potential to Discriminate between High and Low Field Fertility Bulls.

作者信息

Yániz Jesús L, Palacín Inmaculada, Silvestre Miguel A, Hidalgo Carlos Olegario, Tamargo Carolina, Santolaria Pilar

机构信息

BIOFITER Research Group, Institute of Environmental Sciences (IUCA), University of Zaragoza, 22071 Huesca, Spain.

Departamento de Biología Celular, Biología Funcional y Antropología Física, Universidad de Valencia, 46100 Burjassot, Spain.

出版信息

Biology (Basel). 2021 Nov 4;10(11):1135. doi: 10.3390/biology10111135.

Abstract

The objective of the present study was to investigate whether fertility differences in bulls are reflected in variations of sperm quality when analysing only one ejaculate per male. Two experiments were performed. In the first experiment, frozen semen samples from 20 adult bulls were tested; 10 bulls had high field fertility and 10 bulls had low field fertility. Analyses of sperm motility, membrane integrity, and membrane-acrosome integrity with the ISAS3Fun method were performed. Sperm morphometry of the fluorescence sperm subpopulations obtained with the ISAS3Fun method was also analysed. Significant differences between high- and low-fertility groups were only found with the ISAS3Fun technique, specifically in sperm acrosome integrity, the proportion of spermatozoa with an intact acrosome and damaged membrane, and in sperm head width of spermatozoa with intact structures. Discriminant analyses allowed us to correctly classify 90% of sperm samples in their fertility group using sperm quality parameters. Given that only the results obtained with the ISAS3Fun technique were related to bull fertility, we performed a second experiment aimed to validate the efficacy of this technique to detect the acrosomal integrity of bull spermatozoa, comparing them with the conventional FITC-PNA/propidium iodide (PNA/PI) combination under capacitating conditions. The results indicated that the ISAS3Fun combination provided an accurate assessment of both viability and acrosomal integrity for ejaculated spermatozoa, while the PNA/PI combination underestimated the extension of acrosomal damage due to false negatives. It was concluded that the simultaneous assessment of sperm plasma membranes and acrosome integrity with the ISAS3Fun method is precise and seems to have a greater potential to discriminate between high- and low-fertility bulls than more conventional in vitro sperm quality tests.

摘要

本研究的目的是调查在仅分析每头公牛的一次射精时,公牛的生育力差异是否反映在精子质量的变化上。进行了两项实验。在第一个实验中,对20头成年公牛的冷冻精液样本进行了测试;10头公牛具有高田间生育力,10头公牛具有低田间生育力。采用ISAS3Fun方法对精子活力、膜完整性和膜顶体完整性进行了分析。还分析了用ISAS3Fun方法获得的荧光精子亚群的精子形态测量。高生育力组和低生育力组之间的显著差异仅在ISAS3Fun技术中发现,具体表现在精子顶体完整性、顶体完整而膜受损的精子比例以及结构完整的精子头部宽度方面。判别分析使我们能够使用精子质量参数将90%的精子样本正确分类到其生育力组中。鉴于只有用ISAS3Fun技术获得的结果与公牛生育力相关,我们进行了第二个实验,旨在验证该技术检测公牛精子顶体完整性的有效性,并在获能条件下将其与传统的FITC-PNA/碘化丙啶(PNA/PI)组合进行比较。结果表明,ISAS3Fun组合能准确评估射出精子的活力和顶体完整性,而PNA/PI组合由于假阴性而低估了顶体损伤的程度。得出的结论是,用ISAS3Fun方法同时评估精子质膜和顶体完整性是精确的,并且与更传统的体外精子质量测试相比,似乎更有潜力区分高生育力和低生育力的公牛。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d0/8615164/5bcac3136c5b/biology-10-01135-g001.jpg

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